Alzheimer s & Dementia Translational Research & Clinical Interventions · 2021 · 19 citations · 39 references
MedicineNeurologyNeuroscienceAgingMolecular NeurobiologyMolecular NeuroscienceCognitive AgingGenetics Of AgingNeurodegenerative DiseasesNeurodegenerative DisordersNeuropathology Of AgingVascular Cognitive ImpairmentAge-related Brain ChangesAge-related Cognitive Decline GeneticsMild Cognitive Impairment GeneticsTherapeutic Target IdentificationVascular Cognitive Impairment NeuropathologyWhite Matter AbnormalitiesWhite Matter MicrostructureWhite Matter Pathology
Abstract Introduction The pathogenesis of vascular cognitive impairment (VCI) is not fully understood. GPR39, an orphan G‐protein coupled receptor, is implicated in neurological disorders but its role in VCI is unknown. Methods We performed GPR39 immunohistochemical analysis in post mortem brain samples from mild cognitive impairment (MCI) and control subjects. DNA was analyzed for GPR39 single nucleotide polymorphisms (SNPs), and correlated with white matter hyperintensity (WMH) burden on pre mortem magnetic resonance imaging. Results GPR39 is expressed in aged human dorsolateral prefrontal cortex, localized to microglia and peri‐capillary cells resembling pericytes. GPR39–capillary colocalization, and density of GPR39‐expressing microglia was increased in aged brains compared to young. SNP distribution was equivalent between groups; however, homozygous SNP carriers were present only in the MCI group, and had higher WMH volume than wild‐type or heterozygous SNP carriers. Discussion GPR39 may play a role in aging‐related VCI, and may serve as a therapeutic target and biomarker for the risk of developing VCI.
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2020 Alzheimer's disease facts and figures
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Brain infarction and the clinical expression of Alzheimer disease. The Nun Study
David A. Snowdon · JAMA · 1997 · 2K citations
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Catherine N. Hall, Clare Reynell, Bodil Gesslein et al. · Nature · 2014 · 1.9K citations · Full text
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